ClinVar for Gene (Select 57592) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259204	NM_020832.3(ZNF687):c.562G>A (p.Gly188Arg)	ZNF687 (G188R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259203	NM_020832.3(ZNF687):c.3577C>G (p.Leu1193Val)	ZNF687 (L1193V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259202	NM_020832.3(ZNF687):c.3319G>A (p.Gly1107Arg)	ZNF687 (G1107R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259201	NM_020832.3(ZNF687):c.1375G>A (p.Gly459Arg)	ZNF687 (G459R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259200	NM_020832.3(ZNF687):c.2060G>A (p.Gly687Asp)	ZNF687 (G687D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197747	NM_020832.3(ZNF687):c.3635C>T (p.Pro1212Leu)	ZNF687 (P1212L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197745	NM_020832.3(ZNF687):c.3484C>T (p.Arg1162Trp)	ZNF687 (R1162W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197744	NM_020832.3(ZNF687):c.3278C>T (p.Thr1093Met)	ZNF687 (T1093M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197743	NM_020832.3(ZNF687):c.2962A>G (p.Lys988Glu)	ZNF687 (K988E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197742	NM_020832.3(ZNF687):c.2782G>A (p.Glu928Lys)	ZNF687 (E928K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197741	NM_020832.3(ZNF687):c.1682T>C (p.Val561Ala)	ZNF687 (V561A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197740	NM_020832.3(ZNF687):c.1499C>T (p.Ala500Val)	ZNF687 (A500V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197739	NM_020832.3(ZNF687):c.1433C>A (p.Thr478Lys)	ZNF687 (T478K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197738	NM_020832.3(ZNF687):c.1270G>A (p.Val424Met)	ZNF687 (V424M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197737	NM_020832.3(ZNF687):c.1237A>C (p.Met413Leu)	ZNF687 (M413L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197736	NM_020832.3(ZNF687):c.1094T>C (p.Leu365Ser)	ZNF687 (L365S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3064015	NM_020832.3(ZNF687):c.3525G>A (p.Gly1175=)	ZNF687	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3063532	GRCh37/hg19 1q21.1-23.1(chr1:146577511-157155587)x3	ACP6, ADAM15 +263 more	Copy number gain	not specified	GPathogenic
Select item 3062988	GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3	ACP6, ADAM15 +315 more	Copy number gain	not specified	GPathogenic
Select item 3044761	NM_020832.3(ZNF687):c.*10C>G	ZNF687	Single nucleotide variant (3 prime UTR variant)	ZNF687-related disorder	GBenign
Select item 3023163	NM_020832.3(ZNF687):c.1267G>T (p.Ala423Ser)	ZNF687 (A423S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3021446	NM_020832.3(ZNF687):c.2836C>T (p.Arg946Trp)	ZNF687 (R946W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3019654	NM_020832.3(ZNF687):c.2487C>T (p.Cys829=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3017916	NM_020832.3(ZNF687):c.3559G>A (p.Asp1187Asn)	ZNF687 (D1187N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3017271	NM_020832.3(ZNF687):c.3124G>A (p.Glu1042Lys)	ZNF687 (E1042K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3016209	NM_020832.3(ZNF687):c.2295-4C>T	ZNF687	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3012413	NM_020832.3(ZNF687):c.3078-17G>A	ZNF687	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011377	NM_020832.3(ZNF687):c.2780A>G (p.Glu927Gly)	ZNF687 (E927G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3010389	NM_020832.3(ZNF687):c.3648G>A (p.Lys1216=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005276	NM_020832.3(ZNF687):c.2472-18G>T	ZNF687	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004889	NM_020832.3(ZNF687):c.732G>T (p.Lys244Asn)	ZNF687 (K244N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3003621	NM_020832.3(ZNF687):c.2200G>A (p.Val734Ile)	ZNF687 (V734I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3001848	NM_020832.3(ZNF687):c.1403C>T (p.Ala468Val)	ZNF687 (A468V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2998878	NM_020832.3(ZNF687):c.3485G>A (p.Arg1162Gln)	ZNF687 (R1162Q)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2995494	NM_020832.3(ZNF687):c.1600C>T (p.Arg534Cys)	ZNF687 (R534C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2994954	NM_020832.3(ZNF687):c.825C>T (p.Ser275=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2991500	NM_020832.3(ZNF687):c.3158T>C (p.Leu1053Pro)	ZNF687 (L1053P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2991066	NM_020832.3(ZNF687):c.316G>A (p.Gly106Arg)	ZNF687 (G106R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2989490	NM_020832.3(ZNF687):c.3132T>C (p.His1044=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989012	NM_020832.3(ZNF687):c.1129A>G (p.Thr377Ala)	ZNF687 (T377A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2987648	NM_020832.3(ZNF687):c.3557C>T (p.Pro1186Leu)	ZNF687 (P1186L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2987331	NM_020832.3(ZNF687):c.2514C>G (p.His838Gln)	ZNF687 (H838Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2985213	NM_020832.3(ZNF687):c.3220-11C>T	ZNF687	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983865	NM_020832.3(ZNF687):c.1804G>A (p.Val602Ile)	ZNF687 (V602I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2982762	NM_020832.3(ZNF687):c.3643C>T (p.Leu1215Phe)	ZNF687 (L1215F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2979044	NM_020832.3(ZNF687):c.3461G>A (p.Arg1154His)	ZNF687 (R1154H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2978699	NM_020832.3(ZNF687):c.2042A>G (p.Gln681Arg)	ZNF687 (Q681R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2978305	NM_020832.3(ZNF687):c.3077+17G>A	ZNF687	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977713	NM_020832.3(ZNF687):c.2761_2762inv (p.Glu921Ser)	ZNF687 (E921S)	Inversion (missense variant)	not provided	GUncertain significance
Select item 2975181	NM_020832.3(ZNF687):c.1422A>G (p.Gln474=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2974974	NM_020832.3(ZNF687):c.1954G>T (p.Ala652Ser)	ZNF687 (A652S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2974495	NM_020832.3(ZNF687):c.2620C>G (p.Leu874Val)	ZNF687 (L874V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2973798	NM_020832.3(ZNF687):c.2654G>A (p.Arg885His)	ZNF687 (R885H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2971022	NM_020832.3(ZNF687):c.605C>T (p.Ala202Val)	ZNF687 (A202V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2969948	NM_020832.3(ZNF687):c.1448G>A (p.Ser483Asn)	ZNF687 (S483N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2969691	NM_020832.3(ZNF687):c.784T>C (p.Phe262Leu)	ZNF687 (F262L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2968410	NM_020832.3(ZNF687):c.1321G>A (p.Val441Met)	ZNF687 (V441M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2968186	NM_020832.3(ZNF687):c.1804G>C (p.Val602Leu)	ZNF687 (V602L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2967384	NM_020832.3(ZNF687):c.2964+3G>A	ZNF687	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2965118	NM_020832.3(ZNF687):c.2038G>C (p.Glu680Gln)	ZNF687 (E680Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2965082	NM_020832.3(ZNF687):c.2997G>A (p.Glu999=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2963376	NM_020832.3(ZNF687):c.2943C>T (p.His981=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962475	NM_020832.3(ZNF687):c.2471+11G>C	ZNF687	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961955	NM_020832.3(ZNF687):c.687T>G (p.His229Gln)	ZNF687 (H229Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2961867	NM_020832.3(ZNF687):c.3220-4T>A	ZNF687	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2961716	NM_020832.3(ZNF687):c.3675G>A (p.Ala1225=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2960151	NM_020832.3(ZNF687):c.950A>G (p.Asn317Ser)	ZNF687 (N317S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2959754	NM_020832.3(ZNF687):c.2254C>T (p.Arg752Trp)	ZNF687 (R752W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2959023	NM_020832.3(ZNF687):c.1672C>T (p.Arg558Cys)	ZNF687 (R558C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2958464	NM_020832.3(ZNF687):c.1166A>G (p.Gln389Arg)	ZNF687 (Q389R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2957980	NM_020832.3(ZNF687):c.2635-9_2635-7del	ZNF687	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2956360	NM_020832.3(ZNF687):c.2583G>A (p.Pro861=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2956161	NM_020832.3(ZNF687):c.3521A>C (p.Asp1174Ala)	ZNF687 (D1174A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2919526	NM_020832.3(ZNF687):c.1771G>A (p.Val591Ile)	ZNF687 (V591I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2919167	NM_020832.3(ZNF687):c.3558C>T (p.Pro1186=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2918669	NM_020832.3(ZNF687):c.3689G>A (p.Arg1230Gln)	ZNF687 (R1230Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2914893	NM_020832.3(ZNF687):c.1859C>T (p.Ala620Val)	ZNF687 (A620V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2913752	NM_020832.3(ZNF687):c.1698C>T (p.Cys566=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2911622	NM_020832.3(ZNF687):c.2196C>G (p.Pro732=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2909890	NM_020832.3(ZNF687):c.953_967del (p.Asp318_Ser323delinsGly)	ZNF687	Deletion (inframe_indel)	not provided	GUncertain significance
Select item 2909855	NM_020832.3(ZNF687):c.1815C>A (p.Asp605Glu)	ZNF687 (D605E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2907039	NM_020832.3(ZNF687):c.69G>A (p.Ala23=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2903365	NM_020832.3(ZNF687):c.919A>G (p.Ser307Gly)	ZNF687 (S307G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2902966	NM_020832.3(ZNF687):c.1985C>G (p.Pro662Arg)	ZNF687 (P662R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2901236	NM_020832.3(ZNF687):c.1605C>T (p.Cys535=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2900942	NM_020832.3(ZNF687):c.3494G>A (p.Gly1165Asp)	ZNF687 (G1165D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2900347	NM_020832.3(ZNF687):c.1833G>A (p.Pro611=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2899230	NM_020832.3(ZNF687):c.1360G>A (p.Gly454Arg)	ZNF687 (G454R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2898549	NM_020832.3(ZNF687):c.1923CTC[1] (p.Ser643del)	ZNF687 (S643del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2894767	NM_020832.3(ZNF687):c.2079G>A (p.Gln693=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2892877	NM_020832.3(ZNF687):c.2106C>T (p.Ala702=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2891801	NM_020832.3(ZNF687):c.700C>G (p.Leu234Val)	ZNF687 (L234V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888869	NM_020832.3(ZNF687):c.227C>T (p.Pro76Leu)	ZNF687 (P76L)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2888814	NM_020832.3(ZNF687):c.2048G>A (p.Arg683Gln)	ZNF687 (R683Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888444	NM_020832.3(ZNF687):c.2358G>T (p.Ser786=)	ZNF687	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2884987	NM_020832.3(ZNF687):c.2150G>A (p.Arg717His)	ZNF687 (R717H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2883494	NM_020832.3(ZNF687):c.1061A>G (p.Asp354Gly)	ZNF687 (D354G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2882249	NM_020832.3(ZNF687):c.3143G>A (p.Arg1048Gln)	ZNF687 (R1048Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2873326	NM_020832.3(ZNF687):c.3077+13C>T	ZNF687	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2873177	NM_020832.3(ZNF687):c.2965-12C>G	ZNF687	Single nucleotide variant (intron variant)	not provided	GLikely benign

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